Scientific name	Authority	First published in
Vitex esquirolii	H.Lév.	Fl. Kouy-Tchéou : 443 (1915)
Buddleja acuminatissima	Blume	Bijdr. Fl. Ned. Ind. : 743 (1826)
Buddleja amentacea	Kraenzl.	Izv. Imp. Bot. Sada Petra Velikago 13: 92 (1913)
Buddleja arfakensis	Kaneh. & Hatus.	Bot. Mag. (Tokyo) 56: 157 (1942)
Buddleja asiatica var. densiflora	Koord.	Natuurk. Tijdschr. Ned.-Indië 61: 93 1903
Buddleja asiatica var. salicina	Koord.	Natuurk. Tijdschr. Ned.-Indië 61: 93 1903
Buddleja asiatica var. sundaica	Koord.	Natuurk. Tijdschr. Ned.-Indië 61: 93 1903
Buddleja densiflora	Blume	Bijdr. Fl. Ned. Ind. : 743 (1826)
Buddleja discolor	Roth	Nov. Pl. Sp. : 83 (1821)
Buddleja neemda	Buch.-Ham. ex Roxb.	Fl. Ind. 1: 411 (1820)
Buddleja salicina	Lam.	Tabl. Encycl. 1: 291 (1792)
Buddleja serrulata	Roth	Nov. Pl. Sp. : 82 (1821)
Buddleja subserrata	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 92 (1825)
Buddleja sundaica	Blume	Bijdr. Fl. Ned. Ind. : 743 (1826)
Buddleja virgata	Blanco	Fl. Filip. [F.M. Blanco] 57. 1837
Buddleja neemda var. philippensis	Cham. & Schltdl.	Linnaea 2: 598 1827
Buddleja asiatica var. brevicuspe	Koord.
Buddleja asiatica var. densiflora	(Blume) Koord. & Valeton
Buddleja asiatica var. salicina	(Lam.) Koord. & Valeton
Buddleja asiatica var. sundaica	(Blume) Koord. & Valeton

Common names Top

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Filter by language:

Language	Common/alternative name
English	dogtail
Nepali	भिमसेनपाती
Chinese	水黄花
Chinese	扬波
Chinese	白花醉鱼草
Chinese	黄合叶
Chinese	驳骨丹醉鱼草
Chinese	王记叶
Chinese	狭叶醉鱼草
Chinese	白埔姜
Chinese	山埔姜
Chinese	駁骨丹
Chinese	白鱼尾
Chinese	白背枫
Chinese	揚波
Chinese	驳骨丹
Chinese	白鱼尾果
Chinese	七里香

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Taiwan
- Western Asia
  - East Aegean Islands

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - West Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Marianas
- Southwestern Pacific
  - Vanuatu

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000573923
USDA Plants	BUAS
Tropicos	19000533
KEW	urn:lsid:ipni.org:names:545686-1
The Plant List	kew-2685315
Open Tree Of Life	55258
NCBI Taxonomy	69056
Nature Serve	2.140991
IUCN Red List	85520421
IPNI	545686-1
iNaturalist	159585
GBIF	3173333
Freebase	/m/0gvs56h
EPPO	BUDAS
EOL	581488
USDA GRIN	8074
Wikipedia	Buddleja_asiatica

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Changes in Growth and Heavy Metal and Phenolic Compound Accumulation in Buddleja cordata Cell Suspension Culture under Cu, Fe, Mn, and Zn Enrichment

Vazquez-Marquez AM, Bernabé-Antonio A, Correa-Basurto J, Burrola-Aguilar C, Zepeda-Gómez C, Cruz-Sosa F, Nieto-Trujillo A, Estrada-Zúñiga ME

Plants (Basel)

19-Apr-2024

PMCID:	PMC11054087
doi:	10.3390/plants13081147
PMID:	38674556

In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review

Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM

Am J Cancer Res

15-Mar-2024

PMCID:	PMC10998760
doi:	10.62347/AUHB5811
PMID:	38590420

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

Women's wellness in the mountains: An exploration of medicinal plants among tibeto-burman groups in Thailand

Inta A, Kampuansai J, Kutanan W, Srikummool M, Pongamornkul W, Srisanga P, Panyadee P

Heliyon

28-Jun-2023

PMCID:	PMC10395137
doi:	10.1016/j.heliyon.2023.e17722
PMID:	37539171

The Invasive Tradescantia zebrina Affects Litter Decomposition, but It Does Not Change the Lignocellulolytic Fungal Community in the Atlantic Forest, Brazil

Chiba de Castro WA, Vaz GC, da Silva Matos DM, Vale AH, Bueno AC, Fagundes LF, da Costa L, Bonugli Santos RC

Plants (Basel)

30-May-2023

PMCID:	PMC10255722
doi:	10.3390/plants12112162
PMID:	37299140

Characteristics, Isolation Methods, and Biological Properties of Aucubin

Kartini K, Irawan MA, Setiawan F, Jayani NI

Molecules

17-May-2023

PMCID:	PMC10222036
doi:	10.3390/molecules28104154
PMID:	37241895

Antibacterial and Antibiofilm Efficacy and Mechanism of Ginger (Zingiber officinale) Essential Oil against Shewanella putrefaciens

Zhang C, Xie Y, Qiu W, Mei J, Xie J

Plants (Basel)

20-Apr-2023

PMCID:	PMC10140911
doi:	10.3390/plants12081720
PMID:	37111943

Deciphering complex reticulate evolution of Asian Buddleja (Scrophulariaceae): insights into the taxonomy and speciation of polyploid taxa in the Sino-Himalayan region

Yang F, Ge J, Guo Y, Olmstead R, Sun W

Ann Bot

01-Feb-2023

PMCID:	PMC10550280
doi:	10.1093/aob/mcad022
PMID:	36722368

Wood and bark structure in Buddleja: anatomical background of stem morphology

Frankiewicz KE, Chau JH, Baczyński J, Wdowiak A, Oskolski A

AoB Plants

24-Jan-2023

PMCID:	PMC10060081
doi:	10.1093/aobpla/plad003
PMID:	37007612

Exogenous Application of Green Titanium Dioxide Nanoparticles (TiO2 NPs) to Improve the Germination, Physiochemical, and Yield Parameters of Wheat Plants under Salinity Stress

Mustafa N, Raja NI, Ilyas N, Abasi F, Ahmad MS, Ehsan M, Mehak A, Badshah I, Proćków J

Molecules

30-Jul-2022

PMCID:	PMC9370171
doi:	10.3390/molecules27154884
PMID:	35956833

Potential Use of Emerging Technologies for Preservation of Rice Wine and Their Effects on Quality: Updated Review

Pei J, Liu Z, Huang Y, Geng J, Li X, Ramachandra S, Udeshika AA, Brennan C, Tao Y

Front Nutr

23-Jun-2022

PMCID:	PMC9261873
doi:	10.3389/fnut.2022.912504
PMID:	35811939

Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China

Lu Z, Chen H, Lin C, Ou G, Li J, Xu W

J Ethnobiol Ethnomed

21-Jun-2022

PMCID:	PMC9210605
doi:	10.1186/s13002-022-00544-6
PMID:	35729593

Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P

EFSA J

12-May-2022

PMCID:	PMC9096882
doi:	10.2903/j.efsa.2022.7298
PMID:	35592020

Extinction risk of the endemic vascular flora of Kauai, Hawaii, based on IUCN assessments

Rønsted N, Walsh SK, Clark M, Edmonds M, Flynn T, Heintzman S, Loomis A, Lorence D, Nagendra U, Nyberg B, Opgenorth M, Weisenberger L, Williams A, Wolkis D, Wood KR, Keir M

Conserv Biol

18-Apr-2022

PMCID:	PMC9544520
doi:	10.1111/cobi.13896
PMID:	35146804

Bio-Synthesized Nanoparticles in Developing Plant Abiotic Stress Resilience: A New Boon for Sustainable Approach

Kumari S, Khanna RR, Nazir F, Albaqami M, Chhillar H, Wahid I, Khan MI

Int J Mol Sci

18-Apr-2022

PMCID:	PMC9025213
doi:	10.3390/ijms23084452
PMID:	35457269

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6,7-Dihydroxy-7-(hydroxymethyl)-5-methoxy-1,4,4a,5,6,7a-hexahydrocyclopenta[c]pyran-3-one	162987318	Click to see COC1C2CC(=O)OCC2C(C1O)(CO)O	232.23	unknown	https://doi.org/10.1016/J.FITOTE.2005.04.012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4S,5R,8R,9R,13S,14R,17S,18R,21S)-21-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-one	102410611	Click to see CC1(CC2C3(CCC4(C2(C=CC5C4(CCC6C5(CCC(=O)C6(C)CO)C)C)OC3)C)CC1O)C	470.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
(1S,4S,5R,8R,9R,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-one	102410610	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3)(CCC(=O)C6(C)CO)C)C)C)C	454.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
(3S,4R,4aR,6aR,6bS,8aS,12aS,14R,14aR,14bS)-4,8a-bis(hydroxymethyl)-14-methoxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	163012848	Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)CO)O)C)C)OC)C2C1)C)CO)C	488.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbaldehyde	14423516	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C=O)C	440.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
2,3-Dihydroxyolean-12-en-28-oic acid	3694932	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
21-Hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-one	163080816	Click to see CC1(CC2C3(CCC4(C2(C=CC5C4(CCC6C5(CCC(=O)C6(C)CO)C)C)OC3)C)CC1O)C	470.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
4,8a-Bis(hydroxymethyl)-14-methoxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	163012847	Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)CO)O)C)C)OC)C2C1)C)CO)C	488.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
9-(Hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-ol	13322819	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3)(CCC(C6(C)CO)O)C)C)C)C	456.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
9-(Hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-one	162865953	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3)(CCC(=O)C6(C)CO)C)C)C)C	454.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
CID 21594257	21594257	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3)(CCC(C6(C)CO)O)C)C)C)C	456.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
Maslinic Acid	73659	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
Olean-12-en-3beta-ol	225689	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
Oleanolic aldehyde	10321055	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C=O)C	440.70	unknown	https://doi.org/10.1515/ZNB-2008-0717
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(4-Acetyloxy-5,6-dihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate	162975905	Click to see CC1C(C(C(C(O1)O)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC	366.40	unknown	https://doi.org/10.1002/HLCA.200890141
(4,5,6-Trihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate	85101415	Click to see CC1C(C(C(C(O1)O)O)O)OC(=O)C=CC2=CC=C(C=C2)OC	324.32	unknown	https://doi.org/10.1002/HLCA.200890141
(5-Acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate	162924401	Click to see CC1C(C(C(C(O1)O)OC(=O)C)O)OC(=O)C=CC2=CC=C(C=C2)OC	366.40	unknown	https://doi.org/10.1002/HLCA.200890141
[(2S,3R,4R,5R,6R)-5-acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate	102394756	Click to see CC1C(C(C(C(O1)O)OC(=O)C)O)OC(=O)C=CC2=CC=C(C=C2)OC	366.40	unknown	https://doi.org/10.1002/HLCA.200890141
[(2S,3R,4S,5R,6R)-4,5,6-trihydroxy-2-methyloxan-3-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate	10041914	Click to see CC1C(C(C(C(O1)O)O)O)OC(=O)C=CC2=CC=C(C=C2)OC	324.32	unknown	https://doi.org/10.1002/HLCA.200890141
[(2S,3S,4S,5R,6R)-4-acetyloxy-5,6-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate	102394754	Click to see CC1C(C(C(C(O1)O)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC	366.40	unknown	https://doi.org/10.1002/HLCA.200890141
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(3,5-Dihydroxyphenyl)nonan-1-one	49778007	Click to see CCCCCCCCC(=O)C1=CC(=CC(=C1)O)O	250.33	unknown	https://doi.org/10.1002/HLCA.200890141
> Organoheterocyclic compounds / Oxepanes
(1S,4S,5R,8R,9R,14S,17S,18R,21S,22R)-4,5,9,12,12,17,24,24-octamethyl-11,13,28-trioxaheptacyclo[19.5.2.01,22.04,21.05,18.08,17.09,14]octacos-19-ene	163038653	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3)(CCC7C6(COC(O7)(C)C)C)C)C)C)C	496.80	unknown	https://doi.org/10.1515/ZNB-2008-0717
4,5,9,12,12,17,24,24-Octamethyl-11,13,28-trioxaheptacyclo[19.5.2.01,22.04,21.05,18.08,17.09,14]octacos-19-ene	163038652	Click to see CC1(CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1)OC3)(CCC7C6(COC(O7)(C)C)C)C)C)C)C	496.80	unknown	https://doi.org/10.1515/ZNB-2008-0717
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
4-Methoxycinnamic acid	13245	Click to see COC1=CC=C(C=C1)C=CC(=O)O	178.18	unknown	https://doi.org/10.1002/HLCA.200890141
trans-4-Methoxycinnamic acid	699414	Click to see COC1=CC=C(C=C1)C=CC(=O)O	178.18	unknown	https://doi.org/10.1002/HLCA.200890141
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(4-Acetyloxy-5,6-dihydroxy-2-methyloxan-3-yl) 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	162968944	Click to see CC1C(C(C(C(O1)O)O)OC(=O)C)OC(=O)C=CC2=CC(=C(C=C2)O)OC	382.40	unknown	https://doi.org/10.1002/HLCA.200890141
(5-Acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl) 3-(3,4-dimethoxyphenyl)prop-2-enoate	163081558	Click to see CC1C(C(C(C(O1)O)OC(=O)C)O)OC(=O)C=CC2=CC(=C(C=C2)OC)OC	396.40	unknown	https://doi.org/10.1002/HLCA.200890141
[(2S,3R,4R,5R,6R)-5-acetyloxy-4,6-dihydroxy-2-methyloxan-3-yl] (E)-3-(3,4-dimethoxyphenyl)prop-2-enoate	102394755	Click to see CC1C(C(C(C(O1)O)OC(=O)C)O)OC(=O)C=CC2=CC(=C(C=C2)OC)OC	396.40	unknown	https://doi.org/10.1002/HLCA.200890141
3,4-Dimethoxycinnamic acid	717531	Click to see COC1=C(C=C(C=C1)C=CC(=O)O)OC	208.21	unknown	https://doi.org/10.1002/HLCA.200890141
coumaroyl(3-OMe)(-4)a-Rha3Ac	102394753	Click to see CC1C(C(C(C(O1)O)O)OC(=O)C)OC(=O)C=CC2=CC(=C(C=C2)O)OC	382.40	unknown	https://doi.org/10.1002/HLCA.200890141
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1002/HLCA.200890141
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1002/HLCA.200890141 https://doi.org/10.1016/0378-8741(84)90075-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/0378-8741(84)90075-8
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/0378-8741(84)90075-8

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Buddleja asiatica

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